Logo
Analytic Search Group, Princeton NJ

Director of Information Technology

Analytic Search Group, Princeton NJ, Princeton, New Jersey, us, 08543

Save Job

Analytic Search Group, Princeton NJ | Full time

Director of Information Technology Princeton, United States | Posted on 01/13/2026

Industry Pharma/Biotech/Clinical Research

Job Type Full time

State/Province New Jersey

Country United States

Job Description NJ based Clinical Research Org. seeks astrategic,operationally minded, and hands‑on Director of IT to lead and evolve ourinternal technology function across both government and commercial programs. The ideal candidate will be an experienced IT leader who can synthesizetechnical complexity into clear, actionable plans that align with clinical andbusiness goals.

Thisis not a "heads-down" role—it's a leadership position that seeks strategic vision, team oversight, and active engagement in execution. The IT department isundergoingtransformation. This is a unique opportunity where you’llbe responsible for restructuring,mentoring, and rebuilding a high-performing IT organization that can supportour mission‑critical clinical systems and digital reshaping initiatives.

Key Responsibilities

Lead a diverse internal ITteam across five core functions, maintaining visibility into each at astrategic (2,000‑ft) level

Evaluate and restructure thecurrent IT org chart — identify gaps, reassign roles, and optimize FTEsvs. contractors

Build strong partnershipswith clinical and operational teams to ensure IT supports user needs

Guide the migration of systems and databases (Oracle, .NET, Git, etc.) to the cloud and recommend optimal platforms (e.g., evaluating Aurora vs. Oracle)

Oversee the development and validation of programs using technologies such as

C# ,

.NET ,

Oracle ,

MedidataRave , and

SQL

for data extraction, transformation, and loading (ETL).

Direct the creation of high-quality graphical reports and dashboards using

BusinessIntelligence tools , providing actionable insights for clinical trial progress and outcomes.

Direct application development for both internal and external stakeholders, including Clinical Trial Management Systems (CTMS), IWRS/IVRS platforms, and reporting systems ( Power BI, RAVE )

Support

CFR Part11/GxP -compliant systems, focusing on documentation, validation, and specifications

Collaborate on digital transformation and modernization of legacy systems — including redeployment of government-developed tools into commercial use

Ensure proper IT participation in every new client setup, including Medidata and internal systems integration

Quantify, document, and communicate IT’s alignment with business goals

Participate in strategic planning, budgeting, and vendor oversight to ensure ROI and performance from external providers

Qualifications

10+ years

of progressive IT experience, with at least 3 years in a Director or equivalent leadership role

Proven success

managing cross‑functional IT teams

(development, infrastructure, validation, etc.)

Experience in

biotech, life sciences, clinical research, healthcare ,

or regulated environments

In‑depth understanding of clinical trial phases, data flow, and regulatory requirements (e.g.,

CDISC standards, 21 CFR Part 11 ).

Strategic thinker with operational execution skills — able to go from 50,000 feet to ground level as needed

Track record of

change management, team restructuring, and mentoring talent

Strong communication and collaboration skills with technical and non‑technical stakeholders

Background in

hybrid IT environments , ideally across government and commercial projects

#J-18808-Ljbffr